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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454461Generated: October 30, 2026

Dimethylformamide → 7-(Benzyloxy)-2,3-dihydrobenzo[1,4]dioxine-6-carbaldehyde

https://huagongshe.com/reaction/454461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Benzodioxin-6-carboxaldehyde, 2,3-dihydro-7-hydroxy-HCID 14142821—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product7-(Benzyloxy)-2,3-dihydrobenzo[1,4]dioxine-6-carbaldehydeHCID 86659238—

Reaction Conditions

Temperature65 °C

Reaction Steps

Potassium carbonate (0.27 g) and benzyl bromide (0.17 mL) were sequentially added to an N,N-dimethylformamide (2 mL) solution of 7-hydroxy-2,3-dihydrobenzo[1,4]dioxine-6-carbaldehyde (0.23 g), followed by stirring at 65° C. for 2 hours. Benzyl bromide (0.077 mL) was added to the reaction mixture, followed by stirring at 65° C. for 30 minutes. The reaction mixture was cooled to room temperature, and then water and ethyl acetate were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 75-60% hexane/ethyl acetate] to obtain 0.32 g of 7-(benzyloxy)-2,3-dihydrobenzo[1,4]dioxine-6-carbaldehyde as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-94242d7597864bdfac89cfc187dfde9d
Source noteuspto-grants-2013_07